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MRS 1754 - ≥98%, high purity , CAS No.264622-58-4, Antagonist of A 1 receptor;Antagonist of A 2A receptor;Antagonist of A 2B receptor;Antagonist of A 3 receptor

  • Moligand™
  • ≥98%
Item Number
M275233
Grouped product items
SKUSizeAvailabilityPrice Qty
M275233-5mg
5mg
In stock
$151.90
M275233-10mg
10mg
In stock
$205.90
M275233-25mg
25mg
In stock
$423.90
M275233-50mg
50mg
In stock
$763.90

Selective A 2B antagonist

Basic Description

SynonymsMRS 1754|264622-58-4|MRS1754|MRS-1754|N-(4-Cyanophenyl)-2-(4-(2,6-dioxo-1,3-dipropyl-2,3,6,9-tetrahydro-1H-purin-8-yl)phenoxy)acetamide|N-(4-cyanophenyl)-2-[4-(2,6-dioxo-1,3-dipropyl-7H-purin-8-yl)phenoxy]acetamide|7E435V2DAH|CHEMBL273807|N-(4-Cyanophenyl
Specifications & Purity≥98%
Storage TempStore at -20°C,Desiccated
Shipped InDry ice
GradeMoligand™
Action TypeANTAGONIST
Mechanism of actionAntagonist of A 1 receptor;Antagonist of A 2A receptor;Antagonist of A 2B receptor;Antagonist of A 3 receptor
Product Description

MRS 1754 is a selective antagonist radioligand for A2B adenosine receptor with very low affinity for A1 and A3 receptors of both humans and rats。

Associated Targets

CYP3A4 Tclin Cytochrome P450 3A4 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADORA2A Tclin Adenosine receptor A2a 2 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADORA2B Tclin Adenosine receptor A2b 2 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADORA1 Tclin Adenosine receptor A1 2 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADORA3 Tchem Adenosine receptor A3 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name N-(4-cyanophenyl)-2-[4-(2,6-dioxo-1,3-dipropyl-7H-purin-8-yl)phenoxy]acetamide
INCHI InChI=1S/C26H26N6O4/c1-3-13-31-24-22(25(34)32(14-4-2)26(31)35)29-23(30-24)18-7-11-20(12-8-18)36-16-21(33)28-19-9-5-17(15-27)6-10-19/h5-12H,3-4,13-14,16H2,1-2H3,(H,28,33)(H,29,30)
InChi Key AJBBEYXFRYFVNM-UHFFFAOYSA-N
Canonical SMILES CCCN1C2=C(C(=O)N(C1=O)CCC)NC(=N2)C3=CC=C(C=C3)OCC(=O)NC4=CC=C(C=C4)C#N
Isomeric SMILES CCCN1C2=C(C(=O)N(C1=O)CCC)NC(=N2)C3=CC=C(C=C3)OCC(=O)NC4=CC=C(C=C4)C#N
Alternate CAS 264622-58-4
PubChem CID 6603931
MeSH Entry Terms 8-(4-(((4-cyanophenyl)carbamoylmethyl)oxy)phenyl)-1,3-di(ni-propyl)xanthine;MRS 1754;MRS-1754;MRS1754;N-(4-cyanophenyl)-2-(4-(2,3,6,7-tetrahydro-2,6-dioxo-1,3-dipropyl-1H-purin-8-yl)-phenoxy)acetamide
Molecular Weight 486.52

Certificates

Certificate of Analysis(COA)

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4 results found

Lot NumberCertificate TypeDateItem
B2320383Certificate of AnalysisDec 18, 2023 M275233
B2320426Certificate of AnalysisDec 18, 2023 M275233
B2320431Certificate of AnalysisDec 18, 2023 M275233
B2320511Certificate of AnalysisDec 18, 2023 M275233

Chemical and Physical Properties

SolubilitySoluble in DMSO to 50 mM

Safety and Hazards(GHS)

Pictogram(s) GHS07
Signal Warning
Hazard Statements

H302:Harmful if swallowed

Precautionary Statements

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P270:Do not eat, drink or smoke when using this product.

P330:Rinse mouth.

P301+P317:IF SWALLOWED: Get medical help.

Related Documents

References

1. Yi X et al..  (2018)  Adenosine receptors enhance the ATP-induced odontoblastic differentiation of human dental pulp cells..  Biochem Biophys Res Commun,  497  (3): (850-856).  [PMID:29454963]
2. Basu M et al..  (2020)  Increased host ATP efflux and its conversion to extracellular adenosine is crucial for establishing Leishmania infection..  J Cell Sci,  133  (7):   [PMID:32079656]
3. Zhou Y et al..  (2019)  MRS1754 inhibits proliferation and migration of bladder urothelial carcinoma by regulating mitogen-activated protein kinase pathway..  J Cell Physiol,  234  (7): (11360-11368).  [PMID:30565699]

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